[Abstract]Idiopathic pulmonary fibrosis (IPF) is a specific form of chronic, progressive fibrosing interstitial pneumonia of unknown cause, with a poor prognosis. The underlying molecular pathogenic mechanisms are not fully understood. The aim of this study was to investigate the relationship between concentrations of various proteins in bronchoalveolar lavage (BAL) fluid (BALF) and clinical parameters in consecutive patients with IPF, including those with preserved lung function. Concentrations of various proteins (SDF-1α , IP-10, IL-1β , IL-4, IL-6, IL-8, IL-13, IFN-r , TNF-α , EGF, FGF, PDGF, Galectin-3, MMP-1, MMP-7, MMP-8, and TGF-β ) in the BALF collected from ten patients with IPF were determined. As a result, BALF concentrations of ...
SummaryBackgroundEpithelial neutrophil-activating peptide 78 (ENA-78) and interferon γ-inducible pro...
Idiopathic pulmonary fibrosis (IPF) is a chronic lung disease characterized by progressive deteriora...
ponents in the lower respiratory tract of patients with idiopathic pulmonary fibrosis (IPF) and chro...
The proteomic analysis of bronchoalveolar lavage fluid (BALF) can give insight into pulmonary diseas...
Background: Idiopathic pulmonary fibrosis (IPF) is a devastating interstitial lung disease character...
Background: Idiopathic pulmonary fibrosis (IPF) is a devastating interstitial lung disease character...
Background: Idiopathic pulmonary fibrosis (IPF) is a devastating interstitial lung disease character...
Acute exacerbations (AEs) are among the main causes of death in idiopathic pulmonary fibrosis (IPF) ...
Context: Idiopathic pulmonary fibrosis (IPF) and chronic hypersensitivity pneumonitis (HP) are diffu...
Acute exacerbations (AEs) are among the main causes of death in idiopathic pulmonary fibrosis (IPF) ...
Idiopathic pulmonary fibrosis (IPF) is a rare and devastating lung disease of unknown aetiology. Iti...
Various cytokines are known to participate in the pathogenesis of interstitial pneumonia follewed by...
Idiopathic pulmonary fibrosis (IPF) is a rare and devastating lung disease of unknown aetiology. Iti...
Various cytokines are known to participate in the pathogenesis of interstitial pneumonia follewed by...
Various cytokines are known to participate in the pathogenesis of interstitial pneumonia follewed by...
SummaryBackgroundEpithelial neutrophil-activating peptide 78 (ENA-78) and interferon γ-inducible pro...
Idiopathic pulmonary fibrosis (IPF) is a chronic lung disease characterized by progressive deteriora...
ponents in the lower respiratory tract of patients with idiopathic pulmonary fibrosis (IPF) and chro...
The proteomic analysis of bronchoalveolar lavage fluid (BALF) can give insight into pulmonary diseas...
Background: Idiopathic pulmonary fibrosis (IPF) is a devastating interstitial lung disease character...
Background: Idiopathic pulmonary fibrosis (IPF) is a devastating interstitial lung disease character...
Background: Idiopathic pulmonary fibrosis (IPF) is a devastating interstitial lung disease character...
Acute exacerbations (AEs) are among the main causes of death in idiopathic pulmonary fibrosis (IPF) ...
Context: Idiopathic pulmonary fibrosis (IPF) and chronic hypersensitivity pneumonitis (HP) are diffu...
Acute exacerbations (AEs) are among the main causes of death in idiopathic pulmonary fibrosis (IPF) ...
Idiopathic pulmonary fibrosis (IPF) is a rare and devastating lung disease of unknown aetiology. Iti...
Various cytokines are known to participate in the pathogenesis of interstitial pneumonia follewed by...
Idiopathic pulmonary fibrosis (IPF) is a rare and devastating lung disease of unknown aetiology. Iti...
Various cytokines are known to participate in the pathogenesis of interstitial pneumonia follewed by...
Various cytokines are known to participate in the pathogenesis of interstitial pneumonia follewed by...
SummaryBackgroundEpithelial neutrophil-activating peptide 78 (ENA-78) and interferon γ-inducible pro...
Idiopathic pulmonary fibrosis (IPF) is a chronic lung disease characterized by progressive deteriora...
ponents in the lower respiratory tract of patients with idiopathic pulmonary fibrosis (IPF) and chro...